FDA 510(k)

Injection Needle

N.º K: K213914 · 2022-07-29

SolicitanteJiangsu Vedkang Medical Science and Technology Co., Ltd.

Fecha de decisión2022-07-29

Código de productoFBK

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Injection Needle is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Vedkang Medical Science and Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-07-29 under 510(k) number K213914. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Injection Needle?

Injection Needle is a medical device that received FDA 510(k) clearance on 2022-07-29. The listed applicant is Jiangsu Vedkang Medical Science and Technology Co., Ltd.. The 510(k) number is K213914.

When did Injection Needle receive FDA 510(k) clearance?

Injection Needle received FDA 510(k) clearance on 2022-07-29, under 510(k) number K213914.

Who is the listed applicant for Injection Needle?

The FDA 510(k) record lists Jiangsu Vedkang Medical Science and Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Injection Needle?

The FDA product code for Injection Needle is FBK.

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Fuente oficial

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